Department of Chemistry and Medicinal Chemistry Program, Life Sciences Institute, National University of Singapore , 3 Science Drive 3, Republic of Singapore 117543.
Org Lett. 2013 Oct 4;15(19):4920-3. doi: 10.1021/ol402579x. Epub 2013 Sep 25.
With the employment of a threonine-incorporating multifunctional catalyst 9, Michael addition of 3-sulfenyloxindoles to nitroolefins proceeded stereoselectively, leading to the formation of oxindoles with a 3-sulfenyl-substituted quaternary center in excellent yields, and with high diastereoselectivities and excellent enantioselectivities.
采用一种含苏氨酸的多功能催化剂 9,3-亚磺酰氧吲哚与硝基烯烃的迈克尔加成反应具有立体选择性,以高产率、高非对映选择性和优异的对映选择性得到了具有 3-亚磺酰基取代的季碳原子的氧化吲哚。